In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Stromectol Drug Master File in Korea (Stromectol KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Stromectol. The MFDS reviews the Stromectol KDMF as part of the drug registration process and uses the information provided in the Stromectol KDMF to evaluate the safety and efficacy of the drug.
After submitting a Stromectol KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Stromectol API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Stromectol suppliers with KDMF on PharmaCompass.